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Entry Level Clinical Genomic Scientist Jobs (NOW HIRING)

Ambry Genetics

$110K - $114K/yr

Compensation: $110,000-$114,000 annually Clinical Genomics Scientist II - Remote US: Experienced reporting position for individuals, typically genetic counselors or PhD scientists, with clinical ...

MyOme

Clinical Genomic Specialist

Chicago, IL

$110K - $140K/yr

Our team is composed of seasoned entrepreneurs, scientists, and operators, and we're backed by top-tier investors. Position Overview: MyOme is seeking a motivated Clinical Genomic Specialist to ...

Broad Institute

Clinical Genomics Coordinator

Cambridge, MA · On-site

$58K - $76K/yr

Support other projects related to genetic and genomic research at the Broad QUALIFICATIONS: * Qualifications: BA or BS degree in the sciences with 2+ years as a Clinical Genomics Assistant or related ...

Belay Diagnostics

Clinical Genomics Analyst

Chicago, IL · On-site

$80K - $90K/yr

Evaluate variant function, potential clinical impact and genotype-phenotype relationships using scientific literature and available genomic tools * Write clear, communicable reports based on test ...

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Entry Level Clinical Genomic Scientist information

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How much do entry level clinical genomic scientist jobs pay per hour?

As of Jul 26, 2026, the average hourly pay for entry level clinical genomic scientist in the United States is $54.75, according to ZipRecruiter salary data. Most workers in this role earn between $40.14 and $68.27 per hour, depending on experience, location, and employer.

What is the difference between Entry Level Clinical Genomic Scientist vs Entry Level Molecular Laboratory Technician?

AspectEntry Level Clinical Genomic ScientistEntry Level Molecular Laboratory Technician
CredentialsBachelor's degree in genetics, biology, or related field; certification preferredBachelor's degree in biology, chemistry, or related field; certification often not required
Work EnvironmentClinical laboratories, hospitals, research institutionsResearch labs, diagnostic labs, hospitals
Employer & IndustryHealthcare, diagnostics, biotech companiesResearch institutions, diagnostic labs, biotech firms
Common Search & ComparisonYesYes

The Entry Level Clinical Genomic Scientist typically requires specialized knowledge in genomics and often certification, working mainly in clinical settings. In contrast, the Entry Level Molecular Laboratory Technician focuses on laboratory procedures with less emphasis on genomics-specific training. Both roles are essential in healthcare and research, but the genomic scientist role involves more advanced interpretation of genetic data.

What are the key skills and qualifications needed to thrive as an Entry Level Clinical Genomic Scientist, and why are they important?

To thrive as an Entry Level Clinical Genomic Scientist, you need a solid background in genetics, molecular biology, and bioinformatics, typically supported by a bachelor’s or master’s degree in a relevant field. Familiarity with next-generation sequencing (NGS) platforms, data analysis software, and laboratory information management systems (LIMS) is commonly required. Attention to detail, problem-solving abilities, and strong communication skills help ensure accuracy and effective collaboration with clinical teams. These competencies are vital for delivering reliable genomic data and supporting accurate clinical decision-making in healthcare settings.

What types of projects and responsibilities can an entry level clinical genomic scientist expect in their first year?

As an entry level clinical genomic scientist, you will typically assist with genomic data analysis, variant interpretation, and laboratory workflows under the supervision of senior scientists. Your responsibilities may include preparing samples, conducting quality control checks, and helping interpret genetic test results for clinical reports. You’ll often collaborate with laboratory technologists, genetic counselors, and clinicians to ensure accurate and timely data delivery. The first year is focused on building your technical skills and understanding clinical genomics guidelines, which sets a strong foundation for more independent work as you gain experience.

What are entry level clinical genomic scientists?

Entry level clinical genomic scientists are professionals who analyze genetic data to assist in the diagnosis and management of diseases. They typically work in clinical laboratories, hospitals, or research institutions under the supervision of experienced scientists. Their responsibilities include performing genetic tests, interpreting results, maintaining laboratory equipment, and ensuring quality control. This role often serves as a starting point for those who have recently completed a degree in genetics, biology, or a related field and are seeking to gain hands-on experience in clinical genomics.
More about Entry Level Clinical Genomic Scientist jobs
What cities are hiring for Entry Level Clinical Genomic Scientist jobs? Cities with the most Entry Level Clinical Genomic Scientist job openings:
What are the most commonly searched types of Clinical Genomic Scientist jobs? The most popular types of Clinical Genomic Scientist jobs are:
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Entry Level Clinical Genomic Scientist jobs near you
Infographic showing various Entry Level Clinical Genomic Scientist job openings in the United States as of July 2026, with employment types broken down into 81% Full Time, 13% Part Time, and 6% Contract. Highlights an 100% In-person job distribution, with an average salary of $113,877 per year, or $54.7 per hour.
Clinical Genomic Scientist II (genome analyst): REMOTE, USA

Clinical Genomic Scientist II (genome analyst): REMOTE, USA

Ambry Genetics

Remote

$110K - $114K/yr

Full-time

Posted 16 days ago

Job description

Compensation:

$110,000-$114,000 annually

Clinical Genomics Scientist II - Remote US:

Experienced reporting position for individuals, typically genetic counselors or PhD scientists, with clinical laboratory experience.

Responsibilities include:

interpreting diagnostic test results, review and summary of relevant medical literature, and/or review and summary of clinical information. The Clinical Genomic Scientist II is highly proficient in variant classification guidelines and in following report generation protocols to meet requirements for quality and turnaround time. The Clinical Genomic Scientist II has an understanding of genomic technologies and may assist in technical troubleshooting as needed. Additional responsibilities as designated by the Supervisor/Manager, which may include providing input in the development of guidelines and/or assisting with training of new Clinical Genomic Scientists.

Essential Functions:

Attend and provide input at trainings regarding reporting protocols applicable to the specific position or specialty

Leverage awareness of current process and systems to provide suggestions for improvements

Maintain expertise in clinical and technical aspects relevant to the specific position

Interpret clinical diagnostic testing results in accordance with established SOPs

Variant assessment and classification

Independently draft clear, accurate clinical testing results

Effective communication and collaboration with team colleagues; ability to regularly provide input and receive feedback in team discussions

Other duties as assigned

Qualifications:

Ph.D. in Molecular Biology, Genetics, or related scientific field or MS in Genetic Counseling from an accredited institution or MS in Genetics, Molecular Biology, Biochemistry, or other similar field of study

2+ years of experience in at least one of the following areas: primary genetics literature review, variant classification, genetic evidence summary writing, clinical report drafting, or sequencing result analysis

Thorough and ongoing knowledge of current theories and principles of human genetics

Ability to understand and evaluate genetic data and literature

Excellent written and verbal communication skills Enthusiasm and ability to work in and contribute to a fast-paced, highly collaborative environment

Familiarity with diagnostic testing methodologies, including next-generation and Sanger sequencing, microarray, and MLPA

Maintain expertise in clinical and technical aspects related to the specific position and communicate with other internal departments to resolve/ escalate issues as appropriate

Must possess strong working knowledge of human genetics and diagnostic genetic testing concept

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